Prospective Validation of a Pre-Specified Algorithm for the Management of Conduction Disturbances Following TAVR
Recruiting
Observational Study
Conduction Disturbances
Transcatheter Aortic Valve Replacement
Permanent Pacemaker Implantation
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 2,000 (estimated)
- Sponsor
- Centre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Quebec · Other
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About This Trial
The high incidence and variety of conduction disturbances post-TAVR represents a major challenge in the periprocedural management of TAVR recipients. Despite the growing body of knowledge on this topic, the large variability in the management of these complications has translated into a high degree of uncertainty regarding the most appropriate treatment of a large proportion of such patients. The …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
-Patients with aortic valve disease undergoing transcatheter aortic valve replacement
Exclusion Criteria:
* Prior permanent pacemaker
* Failure to provide signed informed consent for data collection
* Impossibility for a follow-up
* Unwillingness to follow the pre-specified st…
Contacts